510(k) K083347 ยท DRL Tester, Defibrillator
IMPULSE 7010 DEFIBRILLATOR SELECTABLE LOADS
| Applicant | Fluke Biomedical, Orange CA, US |
| Decision | Substantially Equivalent, Dec 24, 2008 |
| Received | Nov 13, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083347
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.